A mutation affecting carbon catabolite repression suppresses growth defects in pyruvate carboxylase mutants from Saccharomyces cerevisiae.
Yeasts with disruptions in the genes PYC1 and PYC2 encoding the isoenzymes of pyruvate carboxylase cannot grow in a glucose-ammonium medium (Stucka et al. (1991) Mol. Gen. Genet. 229, 307-315). We have isolated a dominant mutation, BPC1-1, that allows growth in this medium of yeasts with interrupted PYC1 and PYC2 ... genes. The BPC1-1 mutation abolishes catabolite repression of a series of genes and allows expression of the enzymes of the glyoxylate cycle during growth in glucose. A functional glyoxylate cycle is necessary for suppression as a disruption of gene ICL1 encoding isocitrate lyase abolished the phenotypic effect of BPC1-1 on growth in glucose-ammonium. Concurrent expression from constitutive promoters of genes ICL1 and MLS1 (encoding malate synthase) also suppressed the growth phenotype of pyc1 pyc2 mutants. The mutation BPC1-1 is either allelic or closely linked to the mutation DGT1-1.
Mesh Terms:
Alleles, Base Sequence, Carbon, Culture Media, DNA, Fungal, Glucose, Glyoxylates, Isoenzymes, Molecular Sequence Data, Mutation, Phenotype, Pyruvate Carboxylase, Quaternary Ammonium Compounds, Saccharomyces cerevisiae
Alleles, Base Sequence, Carbon, Culture Media, DNA, Fungal, Glucose, Glyoxylates, Isoenzymes, Molecular Sequence Data, Mutation, Phenotype, Pyruvate Carboxylase, Quaternary Ammonium Compounds, Saccharomyces cerevisiae
FEBS Lett.
Date: Dec. 18, 1995
PubMed ID: 8543050
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